Proteinuria and severe mixed dyslipidemia associated with a novel APOAV gene mutation
| Autor: | Robert A. Hegele, Grahame Wood, Paul N. Durrington, Emyr W. Benbow, Ian Roberts, Jian Wang, Handrean Soran, Valentine Charlton-Menys |
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| Rok vydání: | 2010 |
| Předmět: |
Adult
Male Heterozygote medicine.medical_specialty RNA Splicing Endocrinology Diabetes and Metabolism Cardiovascular research Gene mutation Kidney Hyperlipoproteinemia Type III Internal Medicine medicine Humans Obesity Apolipoproteins A Triglycerides Dyslipidemias Nutrition and Dietetics business.industry University hospital medicine.disease humanities Proteinuria Apolipoprotein A-V Family medicine Mutation Cardiology and Cardiovascular Medicine business Dyslipidemia |
| Zdroj: | Journal of Clinical Lipidology. 4:310-313 |
| ISSN: | 1933-2874 |
| DOI: | 10.1016/j.jacl.2010.06.004 |
| Popis: | Cardiovascular Research Group, School of Clinical & Laboratory Sciences, University of Manchester, Core Technology Facility (3 Floor), 46 Grafton Street, Manchester, M13 9NT, United Kingdom (Drs. Soran, Charlton-Menys, and Durrington); Robarts Research Institute, University of West Ontario, Ontario, Canada (Drs. Hegele and Wang); Department of Histopathology, Central Manchester and Manchester Children University Hospitals, Manchester, United Kingdom (Dr. Benbow); Department of Histopathology, John Radcliffe Hospital, Oxford, United Kingdom (Dr. Roberts); and Department of Nephrology, Hope Hospital, Eccles Old Road, Salford M6 8HD, United Kingdom (Dr. Wood) |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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